P792: CRISPR/CAS9-BASED MODEL OF HETEROZYGOUS CXCR4 WT/R334X MUTATION TO STUDY CELLULAR PHENOTYPES IN WHIM SYNDROME

por Zmajkovicova, K., Pawar, S., Maier-Munsa, S., Badarau, A., Taveras, A. G.
Publicado 2022

P793: SCREENING OF NATURALLY OCCURRING CXCR4 VARIANTS FOR IDENTIFICATION OF NOVEL PATHOGENIC MUTATIONS FOR WHIM SYNDROME

por Pawar, S., Wiest, I., Maier-Munsa, S., Maierhofer, B., Sondheimer, N., Taveras, A. G., Badarau, A., Zmajkovicova, K.
Publicado 2022

P1253: MAVORIXAFOR DISRUPTS THE CROSS TALK BETWEEN WALDENSTRÖM’S MACROGLOBULINEMIA CELLS AND THE BONE MARROW MICROENVIRONMENT RESULTING IN ENHANCED SENSITIVITY TO B-CELL TARGETED T...

por Monticelli, H., Kruitwagen, T., Tardelli, M., Rebelo, T., Maierhofer, B., Maier-Munsa, S., Zmajkovicova, K., Taveras, A. G., Nguyen, C.
Publicado 2022